Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss.
MARVELD2 的分子遗传学和巴基斯坦和斯洛伐克家族中 DFNB49 听力损失的临床表型
期刊:Human Genetics
影响因子:3.6
doi:10.1007/s00439-015-1532-y
Nayak Gowri, Varga Lukas, Trincot Claire, Shahzad Mohsin, Friedman Penelope L, Klimes Iwar, Greinwald John H Jr, Riazuddin S Amer, Masindova Ivica, Profant Milan, Khan Shaheen N, Friedman Thomas B, Ahmed Zubair M, Gasperikova Daniela, Riazuddin Sheikh, Riazuddin Saima
